Vaccine Research Section, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, Rockville, MD 20850, USA.
Vaccine. 2011 Jun 6;29(25):4210-7. doi: 10.1016/j.vaccine.2011.03.102. Epub 2011 Apr 16.
There is no licensed vaccine available against Moraxella catarrhalis, an exclusive human pathogen responsible for otitis media in children and respiratory infections in adults. We previously developed conjugate vaccine candidates based on lipooligosaccharides (LOSs) of M. catarrhalis serotypes A, B, and C, each of which was shown to cover a portion of the clinical strains. To generate conserved LOS antigens and eliminate a potential autoimmune response to a similar epitope between M. catarrhalis LOS moiety Galα1-4Galβ1-4Glc and human P(k) antigen, two LOS mutants from strain O35E were constructed. Mutant O35Elgt5 or O35EgalE revealed a deletion of one or two terminal galactose residues of wild type O35E LOS. Each LOS molecule was purified, characterized, detoxified, and coupled to tetanus toxoid (TT) to form conjugates, namely dLOS-TT. Three subcutaneous immunizations using dLOS-TT from O35Elgt5 or O35EgalE elicited significant increases (a 729- or 1263-fold above the preimmune serum levels) of serum immunoglobulin (Ig)G against O35E LOS in rabbits with an adjuvant or without an adjuvant (an 140- or 140-fold above the preimmune serum levels). Rabbit antisera demonstrated elevated complement-mediated bactericidal activities against the wild type strain O35E. The rabbit sera elicited by O35Elgt5 dLOS-TT were further examined and showed cross bactericidal activity against all additional 19 M. catarrhalis strains and clinical isolates studied. Moreover, the rabbit sera displayed cross-reactivity not only among three serotype strains but also clinical isolates in a whole-cell enzyme-linked immunosorbent assay (ELISA), which was further confirmed under transmission electron microscopy. In conclusion, O35Elgt5 dLOS-TT may act as a vaccine against most M. catarrhalis strains and therefore can be used for further in vivo efficacy studies.
目前尚无针对卡他莫拉菌的许可疫苗,卡他莫拉菌是一种专性人类病原体,可导致儿童中耳炎和成人呼吸道感染。我们之前基于卡他莫拉菌血清型 A、B 和 C 的脂寡糖 (LOS) 开发了结合疫苗候选物,每种候选物都能覆盖部分临床分离株。为了产生保守的 LOS 抗原并消除卡他莫拉菌 LOS 部分 Galα1-4Galβ1-4Glc 与人类 P(k) 抗原之间类似表位的潜在自身免疫反应,我们构建了来自 O35E 菌株的两种 LOS 突变体。突变体 O35Elgt5 或 O35EgalE 显示出野生型 O35E LOS 中一个或两个末端半乳糖残基的缺失。每个 LOS 分子均经过纯化、表征、解毒,并与破伤风类毒素 (TT) 结合形成缀合物,即 dLOS-TT。使用 O35Elgt5 或 O35EgalE 的 dLOS-TT 进行三次皮下免疫,可使兔子血清中针对 O35E LOS 的免疫球蛋白 (Ig)G 显著增加(比免疫前血清水平高 729 倍或 1263 倍),且在佐剂或无佐剂的情况下(比免疫前血清水平高 140 倍或 140 倍)。兔抗血清对野生型 O35E 菌株表现出升高的补体介导的杀菌活性。进一步检查 O35Elgt5 dLOS-TT 诱导的兔血清,发现其对研究的所有其他 19 株卡他莫拉菌菌株和临床分离株具有交叉杀菌活性。此外,兔血清不仅在三种血清型菌株之间,而且在全细胞酶联免疫吸附试验 (ELISA) 中也显示出与临床分离株的交叉反应性,这在透射电子显微镜下得到了进一步证实。总之,O35Elgt5 dLOS-TT 可作为针对大多数卡他莫拉菌菌株的疫苗,因此可用于进一步的体内疗效研究。